ClinVar Miner

Submissions for variant NM_004333.6(BRAF):c.1141-18A>G

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003654689 SCV004526648 likely benign RASopathy 2023-01-15 criteria provided, single submitter clinical testing

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